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3.
Rev Clin Esp (Barc) ; 216(2): 108-9, 2016 Mar.
Artículo en Inglés, Español | MEDLINE | ID: mdl-26454614
9.
An Esp Pediatr ; 47(4): 398-404, 1997 Oct.
Artículo en Español | MEDLINE | ID: mdl-9499310

RESUMEN

OBJECTIVE: We report the results of survival and incidence of neurodevelopmental sequelae in a group of 249 infants treated in our hospital between 1986-91, whose birth weight was under 1,500 grams. METHOD: We perform a follow-up at corrected ages of 3, 6, 10, 18, 36 months and 5 years thought results only included children followed until 18. Sequelae were classified in three groups, according to the disability degree. RESULTS: Survival resulted to be 69.87% (174), 38.7% for the group under 1,000 grams and 84.7% for those over 1,000 grams. Sequelae were present in 22.6% (11.6% moderate and 10.9% severe). The incidence of severe sequelae was very different on basis of the birth weight, 25.8% for children under 1,000 grams, 13.9% for 1,000-1,249 grams and 1.6% for 1,250-1,500 grams. CONCLUSIONS: Intracranial haemorrhage, hyperbilirubinemia, assisted ventilation and persistence of ductus arteriosus were significantly associated sequelae. We didn't find differences with respect to multiple pregnancy, seizures, sepsis or neonatal hypoxia.


Asunto(s)
Recién Nacido de muy Bajo Peso , Femenino , Estudios de Seguimiento , Edad Gestacional , Humanos , Recién Nacido , Enfermedades del Recién Nacido/epidemiología , Embarazo , Pronóstico , Estudios Retrospectivos
10.
An Esp Pediatr ; 34(4): 305-9, 1991 Apr.
Artículo en Español | MEDLINE | ID: mdl-2069281

RESUMEN

Three cases of congenital dwarfism are presented. All of them are lethal and represent the three better known nonviable nosologic entities: Achondrogenesis I, Achondrogesis II and Thanatophoric dwarfism. According to clinical features and radiologic data it is possible to approach the diagnosis accurately. We comment genetic, clinic, radiologic and histologic aspects of these processes. It is important to establish a differential diagnosis as these entities have different genetic basis, what influences genetic counsel.


Asunto(s)
Acondroplasia/genética , Osteocondrodisplasias/genética , Displasia Tanatofórica/genética , Acondroplasia/clasificación , Acondroplasia/diagnóstico por imagen , Acondroplasia/mortalidad , Femenino , Asesoramiento Genético , Humanos , Recién Nacido , Masculino , Osteocondrodisplasias/clasificación , Osteocondrodisplasias/diagnóstico por imagen , Osteocondrodisplasias/mortalidad , Diagnóstico Prenatal , Radiografía , Displasia Tanatofórica/clasificación , Displasia Tanatofórica/diagnóstico por imagen , Displasia Tanatofórica/mortalidad
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